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Continuous
Fractionation of DNA Using Asymmetrical Pulsed Field Electrophoresis on Micro/Nano-Fabricated Matrices
Method for Applying Two-Dimensional
Electric Field Distributions in Micro-Electrophoretic
Devices and Injecting Narrow Bands of Samples
Method for Applying Two-Dimensional
Flow Distributions in Micro-Fluidic Devices and Injecting Narrow Bands of
Samples
Researchers
at
The first
method permits fractionation of DNA continuously on micro or nano-fabricated support materials. Current methods to fractionate larger
(greater than 30kb) DNA molecules by size use pulsed gel electrophoresis and
typically take several days to fractionate one set of samples. This new method uses micro or nano fabricated environments to accurately control the
motion of the DNA molecules, allowing continuous fractionation with very high
resolution in a matter of seconds, even for DNA molecules larger than 100kbp.
The second
method permits generation of a wide variety of electrical field distributions
in the electrolyte layer of micro-fabricated electrophoretic
devices. Pulsed field gel
electrophoresis, which is currently used to fractionate large DNA molecules,
requires a uniform, homogeneous alternate electric field. This is performed in standard
electrophoresis setups using multiple electrodes, however, this method is not
practical in microfluidic applications as it requires
a multitude of electrodes, electrolyte reservoirs, complex driving circuits,
and can create undesirable bubbles at the electrode/electrolyte interface. This new method permits the
generation of many types of electrical fields, while minimizing bubble
generation and the number of electrodes, thereby increasing the reliability of
such microfluidic devices.
The third
method allows the generation of a wide variety of flow distributions of a layer
of liquid in micro-fluidic devices.
Current methods require the use of numerous pressure regulators to
control the flow distribution in a layer of liquid, and may not be practical in
microfluidic applications, due to complexity,
instability and cost. This new
method employs pressure sources in series with microfluidic
channels to generate two-dimensional flow distributions.
It is
anticipated that these methods will be useful in any application using
microfluidics or lab-on-a-chip technologies. Patent protection is pending.